Porous-Organic-Polymer-Triggered Advancement of Sustainable Magnetic Efficient Catalyst for Chemoselective Hydrogenation of Cinnamaldehyde

被引:32
作者
Paul, Ratul [1 ]
Sarkar, Chitra [1 ]
Yan, Yong [2 ,3 ]
Trinh, Quang Thang [3 ]
Rao, Bolla Srinivasa [1 ]
Pao, Chih-Wen [4 ]
Lee, Jyh-Fu [4 ]
Liu, Wen [2 ,3 ]
Mondal, John [1 ]
机构
[1] CSIR Indian Inst Chem Technol, Catalysis & Fine Chem Div, Uppal Rd, Hyderabad 500007, Andhra Pradesh, India
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
[3] Campus Res Excellence & Technol Enterprise CREATE, Cambridge Ctr Adv Res & Educ Singapore CARES, 1 Create Way, Singapore 138602, Singapore
[4] Natl Synchrotron Radiat Res Ctr, 101 Hsin Ann Rd, Hsinchu 30076, Taiwan
基金
新加坡国家研究基金会;
关键词
Porous-Organic-Polymer (POP); Cinnamaldehyde hydrogenation; Terephthaldehyde; Magnetic Nanocatalyst; Density Functional Theory (DFT) calculations; SELECTIVE HYDROGENATION; PALLADIUM NANOPARTICLES; SURFACE-CHEMISTRY; CINNAMYL ALCOHOL; ADSORPTION; ACID; HYDROGENOLYSIS; PERFORMANCE; ALPHA-FE2O3; CAPTURE;
D O I
10.1002/cctc.202000072
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we adopted a cost-effective, facile and metal & template-free strategy for the successful synthesis of hydroxyl enriched POP (denoted as TPT). An integrated catalyst, Pd-Fe3O4@TPT, has been developed for the liquid phase selective hydrogenation cinnamaldehyde (CAL). Pd-Fe3O4@TPT exhibited excellent catalytic performance, providing 100 % selectivity towards hydrocinnamaldehyde (HCAL) under mild reaction conditions (with relatively low hydrogen pressure and very short reaction time), whereas Fe2O3@TPT appeared inert. Compared with the conventional catalytic systems, our newly designed catalyst was superior in many aspects, owing to the rigid nature of TPT-POP, which prevents aggregation and leaching of the metal nanoparticles.
引用
收藏
页码:3687 / 3704
页数:18
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